Thomas Scholl

5.2k citations
46 papers · 2.5k · 1 hit paper · h-index 20

Impact in

  • Genetics top 2%
    • BRCA gene mutations in cancer
    • Neurogenetic and Muscular Disorders Research
    • Genomic variations and chromosomal abnormalities
    • Cancer Genomics and Diagnostics

Papers in

    • CRISPR and Genetic Engineering 7
    • RNA and protein synthesis mechanisms 4
    • BRCA gene mutations in cancer 10
    • Genomic variations and chromosomal abnormalities 7

Thomas Scholl

46 papers receiving 2.5k citations

Thomas Scholl's Hit Papers

Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens 2011 · 462 citations
4620+5+10Years since publication100200300400

Peers

Thomas Scholl
Comparison fields: 5 of 110
  • Genetics 452
  • Genetics 943
  • Cancer Research 267
  • Pathology and Forensic Medicine 254
  • Molecular Biology 887
Replace Isamu Hayata with:
Isamu Hayata Japan
P. Meera Khan Netherlands
Patricia Tippett United Kingdom
V. N. Rao United States
Fréderic Morel France
Peggy Beer‐Romero United States
Benjamin Margolis United States
Lise Lotte Hansen Denmark
Laura Cremonesi Italy
Rebecca Shepherd United Kingdom
Thomas Scholl relative to Isamu Hayata Japan Isamu Hayata's profile →
Citations per field
00.5×3.7×
Isamu Hayata · 1×
Citations per year

Countries citing papers authored by Thomas Scholl

Since Specialization
Citations

This map shows the geographic impact of Thomas Scholl's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Thomas Scholl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Scholl more than expected).

Fields of papers citing papers by Thomas Scholl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas Scholl. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Thomas Scholl. The network helps show where Thomas Scholl may publish in the future.

Co-authors

The 25 scholars most cited alongside Thomas Scholl, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Thomas Scholl Line = papers co-authored together Thomas Scholl links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 46 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens
Hit paper breakdown →
2011462
2 2002456
3 2009278
4 2015179
5 2006136
6 1997130
7 2003123
8 1997107
9 200977
10 200869
11 201155
12 200552
13 200543
14 200740
15 199639
16 199431
17 198225
18 198923
19 199920
20 199219

About Thomas Scholl

Thomas Scholl is a scholar working on Molecular Biology, Genetics, Organic Chemistry, Immunology and Pathology and Forensic Medicine, having authored 46 papers that have together received 2.5k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genomic variations and chromosomal abnormalities (7 papers), CRISPR and Genetic Engineering (7 papers), T-cell and B-cell Immunology (5 papers), Immune Cell Function and Interaction (5 papers), RNA and protein synthesis mechanisms (4 papers), Genetic factors in colorectal cancer (4 papers) and Porphyrin and Phthalocyanine Chemistry (3 papers). The work is most often cited by research in Genetics (452 citations), Genetics (943 citations), Cancer Research (267 citations), Pathology and Forensic Medicine (254 citations) and Molecular Biology (887 citations). Thomas Scholl has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Brian E. Ward, Amie M. Deffenbaugh, Jack L. Strominger, S. Mahanta, Julia Reid, Viatcheslav R. Akmaev, Brant C. Hendrickson, Dmitry Pruss, Elizabeth M. Rohlfs and Bernice A. Allitto. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Molecular Diagnostics, Molecular Genetics and Metabolism, Journal of Clinical Oncology and Cancer Research.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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